Philips recalls C9-2 Transducer Probes with specific model numbers for clarification on useful life in the field. No safety risk, but labeling updates required.
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Philips is recalling certain C9-2 Transducer Probes to clarify their useful life in the field. This is a labeling update, not a safety hazard. The product remains safe to use but needs updated labeling information.
The recall is for labeling clarification to define the useful life of the transducers in the field. There is no safety hazard or risk of injury; this is a routine update to help users understand the product's expected lifespan.
Users of Philips C9-2 Transducer Probes with the listed model numbers are affected. This recall does not pose a safety risk but requires labeling updates.
Check your C9-2 Transducer Probe for model numbers: 989605391092, 989605438431, 989605418552, 989605391091, 989605412042, or UDI codes listed in the recall notice.
Look for model numbers on your C9-2 Transducer Probe: 989605391092, 989605438431, 989605418552, 989605391091, 989605412042, or UDI codes listed in the recall notice.
No, this recall is for labeling clarification to define the useful life of the transducers in the field. There is no safety risk.
No, the product remains safe to use. This is a labeling update, not a safety hazard.
No action is needed. The recall requires updated labeling information, but the product is safe to continue using.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2360-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-2360-2025 from Philips. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
